IBM Research Nanophysics Breakthrough Captures First-Ever Image of Charge Distribution in a Single Molecule
by Guest Post on February 27th, 2012
– Scientists use special kind of atomic force microscopy at low temperatures and in ultrahigh vacuum to image the charge distribution within a single molecule
– The new technique will further the understanding of nanoscale physics and could help develop future applications such as solar photoconversion, energy storage, or molecular scale computing devices
ZURICH – 27 Feb 2012: IBM scientists were able to measure for the first time how charge is distributed within a single molecule. This breakthrough will enable fundamental scientific insights into single-molecule switching and bond formation between atoms and molecules. The ability to image the charge distribution within functional molecular structures holds great promise for future applications such as solar photoconversion, energy storage, or molecular scale computing devices.
As reported recently in the journal Nature Nanotechnology, scientists Fabian Mohn, Leo Gross, Nikolaj Moll and Gerhard Meyer of IBM Research succeeded in imaging the charge distribution within a single molecule by using a special kind of atomic force microscopy called Kelvin probe force microscopy at low temperatures and in ultrahigh vacuum.
“This work demonstrates an important new capability of being able to directly measure how charge arranges itself within an individual molecule,” states Michael Crommie, Professor in the Department of Physics at the University of California, Berkeley. “Understanding this kind of charge distribution is critical for understanding how molecules work in different environments. I expect this technique to have an especially important future impact on the many areas where physics, chemistry, and biology intersect.”
The new technique provides complementary information about the molecule, showing different properties of interest. This is reminiscent of medical imaging techniques such as X-ray, MRI, or ultrasonography, which yield complementary information about a person’s anatomy and health condition.
The discovery could be used to study charge separation and charge transport in so-called charge-transfer complexes. These consist of two or more molecules and hold tremendous promise for applications such as computing, energy storage or photovoltaics. In particular, the technique could contribute to the design of molecular-sized transistors that enable more energy efficient computing devices ranging from sensors to mobile phones to supercomputers.
“This technique provides another channel of information that will further our understanding of nanoscale physics. It will now be possible to investigate at the single-molecule level how charge is redistributed when individual chemical bonds are formed between atoms and molecules on surfaces,” explains Fabian Mohn of the Physics of Nanoscale Systems group at IBM Research – Zurich. “This is essential as we seek to build atomic and molecular scale devices.”
Gerhard Meyer, a senior IBM scientist who leads the scanning tunneling microscopy (STM) and atomic force microscopy (AFM) research activities at IBM Research – Zurich adds, “The present work marks an important step in our long term effort on controlling and exploring molecular systems at the atomic scale with scanning probe microscopy.”
For his outstanding work in the field, Meyer recently received a European Research Council Advanced Grant. These prestigious grants support “the very best researchers working at the frontiers of knowledge” in Europe.*
Taking a closer look
To measure the charge distribution, IBM scientists used an offspring of AFM called Kelvin probe force microscopy (KPFM).
When a scanning probe tip is placed above a conductive sample, an electric field is generated due to the different electrical potentials of the tip and the sample. With KPFM this potential difference can be measured by applying a voltage such that the electric field is compensated. Therefore, KPFM does not measure the electric charge in the molecule directly, but rather the electric field generated by this charge. The field is stronger above areas of the molecule that are charged, leading to a greater KPFM signal. Furthermore, oppositely charged areas yield a different contrast because the direction of the electric field is reversed. This leads to the light and dark areas in the micrograph (or red and blue areas in colored ones).
Naphthalocyanine, a cross-shaped symmetric organic molecule which was also used in IBM’s single-molecule logic switch**, was found to be an ideal candidate for this study. It features two hydrogen atoms opposing each other in the center of a molecule measuring only two nanometers in size. The hydrogen atoms can be switched controllably between two different configurations by applying a voltage pulse. This so-called tautomerization affects the charge distribution in the molecule, which redistributes itself between opposing legs of the molecules as the hydrogen atoms switch their locations.
Using KPFM, the scientists managed to image the different charge distributions for the two states. To achieve submolecular resolution, a high degree of thermal and mechanical stability and atomic precision of the instrument was required over the course of the experiment, which lasted several days.
Moreover, adding just a single carbon monoxide molecule to the apex of the tip enhanced the resolution greatly. In 2009, the team has already shown that this modification of the tip allowed them to resolve the chemical structures of molecules with AFM. The present experimental findings were corroborated by first-principle density functional theory calculations done by Fabian Mohn together with Nikolaj Moll of the Computational Sciences group at IBM Research – Zurich.
The scientific paper entitled “Imaging the charge distribution within a single molecule” by F. Mohn, L. Gross, N. Moll, and G. Meyer was published online in Nature Nanotechnology, DOI: 10.1038/NNANO.2012.20 (26 February 2012).
* cited from the ERC press release, January 24, 2012: http://erc.europa.eu/sites/default/files/press_release/files/press_release_adg2011_results.pdf
** P. Liljeroth, J. Repp, and G. Meyer, “Current-Induced Hydrogen Tautomerization and Conductance Switching of Naphthalocyanine Molecules”, Science 317, p.1203–1206 (2007), DOI: 10.1126/science.1144366